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Combined cytotoxic chemotherapy and immunotherapy of cancer: modern times.癌症的细胞毒性化疗与免疫疗法联合应用:现代进展
NAR Cancer. 2020 Feb 17;2(1):zcaa002. doi: 10.1093/narcan/zcaa002. eCollection 2020 Mar.
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Randomized Trial of Irinotecan and Cetuximab With or Without Vemurafenib in BRAF-Mutant Metastatic Colorectal Cancer (SWOG S1406).随机试验伊立替康和西妥昔单抗与或无维莫非尼在 BRAF 突变转移性结直肠癌(SWOG S1406)。
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Neoadjuvant immunotherapy leads to pathological responses in MMR-proficient and MMR-deficient early-stage colon cancers.新辅助免疫治疗导致 MMR 功能正常和 MMR 缺陷的早期结肠癌发生病理应答。
Nat Med. 2020 Apr;26(4):566-576. doi: 10.1038/s41591-020-0805-8. Epub 2020 Apr 6.
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Is There an Optimal Choice in Refractory Colorectal Cancer? A Network Meta-Analysis.复发性结直肠癌的最佳选择是什么?一项网状荟萃分析。
Clin Colorectal Cancer. 2020 Jun;19(2):82-90.e9. doi: 10.1016/j.clcc.2019.10.001. Epub 2020 Mar 17.
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Larotrectinib in patients with TRK fusion-positive solid tumours: a pooled analysis of three phase 1/2 clinical trials.拉罗替尼治疗 TRK 融合阳性实体瘤患者的疗效:三项 I/II 期临床试验的汇总分析。
Lancet Oncol. 2020 Apr;21(4):531-540. doi: 10.1016/S1470-2045(19)30856-3. Epub 2020 Feb 24.
6
TAS-102 with or without bevacizumab in patients with chemorefractory metastatic colorectal cancer: an investigator-initiated, open-label, randomised, phase 2 trial.替拉扎唑联合或不联合贝伐珠单抗治疗化疗耐药转移性结直肠癌患者的疗效:一项研究者发起的、开放标签、随机、2 期临床试验。
Lancet Oncol. 2020 Mar;21(3):412-420. doi: 10.1016/S1470-2045(19)30827-7. Epub 2020 Jan 27.
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Entrectinib in patients with advanced or metastatic NTRK fusion-positive solid tumours: integrated analysis of three phase 1-2 trials.恩曲替尼治疗晚期或转移性 NTRK 融合阳性实体瘤患者的疗效:三项 I/II 期临床试验的整合分析。
Lancet Oncol. 2020 Feb;21(2):271-282. doi: 10.1016/S1470-2045(19)30691-6. Epub 2019 Dec 11.
8
Carcinoembryonic antigen-targeted photodynamic therapy in colorectal cancer models.结直肠癌模型中癌胚抗原靶向光动力疗法
EJNMMI Res. 2019 Dec 11;9(1):108. doi: 10.1186/s13550-019-0580-z.
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TRK inhibitors in TRK fusion-positive cancers.TRK 抑制剂在 TRK 融合阳性癌症中的应用。
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10
Decreased percentage of neutrophil is a predict factor for the efficacy of trifluridine and tipiracil hydrochloride for pretreated metastatic colorectal cancer.中性粒细胞百分比降低是曲氟尿苷和盐酸替匹嘧啶治疗经治转移性结直肠癌疗效的预测因素。
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难治性转移性结直肠癌:当前挑战与未来展望

Refractory Metastatic Colorectal Cancer: Current Challenges and Future Prospects.

作者信息

Lam Marissa, Lum Caroline, Latham Sarah, Tipping Smith Sam, Prenen Hans, Segelov Eva

机构信息

Department of Medical Oncology, Monash Medical Center, Clayton, Australia.

Department of Oncology, University Hospital Antwerp, Edegem, Belgium.

出版信息

Cancer Manag Res. 2020 Jul 15;12:5819-5830. doi: 10.2147/CMAR.S213236. eCollection 2020.

DOI:10.2147/CMAR.S213236
PMID:32765085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7369412/
Abstract

Despite advances, patients with metastatic colorectal cancer (mCRC) still have poor long-term survival. Identification of molecular subtypes is important to guide therapy through standard treatment pathways and holds promise for the development of new treatments. Following standard first- and second-line chemotherapy plus targeted agents, many patients retain a reasonable performance status, and thus are seeking further effective treatment to extend life and maintain symptom control. The challenge lies in selecting the most appropriate therapy in the third- and fourth-line settings, from a range of options including the relatively new oral agents TAS-102 and regorafenib, or rechallenge with previous chemotherapy or anti-epidermal growth factor receptor (anti-EGFR) monoclonal antibodies (mAB). Beyond this, therapy consists of trials involving novel agents and new combinations of treatments with theoretical synergy and/or non-overlapping toxicity. There is a great focus on enhancing immunogenicity in mCRC, to reflect the impressive results of immunotherapy drugs in the small cohort with mismatch repair deficient (dMMR) mCRC. Rare molecular subtypes of mCRC are increasingly being identified, including -positive disease, fusions and others. Clinical trials exploring the efficacy of immunomodulatory and precision agents are plentiful and will hopefully yield clinically meaningful results that can be rapidly translated into routine care.

摘要

尽管取得了进展,但转移性结直肠癌(mCRC)患者的长期生存率仍然很低。识别分子亚型对于通过标准治疗途径指导治疗很重要,并且有望开发新的治疗方法。在接受标准的一线和二线化疗加靶向药物治疗后,许多患者仍保持合理的身体状况,因此正在寻求进一步的有效治疗以延长生命并维持症状控制。挑战在于在三线和四线治疗中,从一系列选择中选择最合适的治疗方法,这些选择包括相对较新的口服药物TAS-102和瑞戈非尼,或重新使用先前的化疗药物或抗表皮生长因子受体(anti-EGFR)单克隆抗体(mAB)。除此之外,治疗还包括涉及新型药物以及具有理论协同作用和/或非重叠毒性的新治疗组合的试验。人们非常关注增强mCRC的免疫原性,以反映免疫治疗药物在错配修复缺陷(dMMR)mCRC小队列中的令人印象深刻的结果。越来越多的mCRC罕见分子亚型被发现,包括 -阳性疾病、融合等。探索免疫调节和精准药物疗效的临床试验很多,有望产生具有临床意义的结果,并能迅速转化为常规治疗。